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A111379-1gAsiatic acid is a pentacyclic triterpene that is known to have anti-inflammatory properties. It stimulates wound healing by increasing collagen production.Starting material for asiatic acid derivative synthesis for use as:· Anticancer agents·
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A111379-200mgAsiatic acid is a pentacyclic triterpene that is known to have anti-inflammatory properties. It stimulates wound healing by increasing collagen production.Starting material for asiatic acid derivative synthesis for use as:· Anticancer agents·
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A111379-50mgAsiatic acid is a pentacyclic triterpene that is known to have anti-inflammatory properties. It stimulates wound healing by increasing collagen production.Starting material for asiatic acid derivative synthesis for use as:· Anticancer agents·
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A111379-5gAsiatic acid is a pentacyclic triterpene that is known to have anti-inflammatory properties. It stimulates wound healing by increasing collagen production.Starting material for asiatic acid derivative synthesis for use as:· Anticancer agents·
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A648206-10mgAsimadoline (EMD-61753) hydrochloride is an orally active, selective and peripherally active κ-opioid agonist with IC 50 s of 5.6 nM (guinea pig) and 1.2 nM (human recombinant). Asimadoline hydrochloride has low permeability across the blood brain
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A648206-25mgAsimadoline (EMD-61753) hydrochloride is an orally active, selective and peripherally active κ-opioid agonist with IC 50 s of 5.6 nM (guinea pig) and 1.2 nM (human recombinant). Asimadoline hydrochloride has low permeability across the blood brain
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A648206-5mgAsimadoline (EMD-61753) hydrochloride is an orally active, selective and peripherally active κ-opioid agonist with IC 50 s of 5.6 nM (guinea pig) and 1.2 nM (human recombinant). Asimadoline hydrochloride has low permeability across the blood brain
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A655341-1mlAsimadoline (EMD-61753) hydrochloride is an orally active, selective and peripherally active κ-opioid agonist with IC 50 s of 5.6 nM (guinea pig) and 1.2 nM (human recombinant). Asimadoline hydrochloride has low permeability across the blood brain
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A648376-10mgASK1-IN-2 is a potent and orally active inhibitor of apoptosis signal-regulating kinase 1 (ASK1) , with an IC 50 of 32.8 nM. ASK1-IN-2 can be used for the research of ulcerative colitisIn VitroASK1-IN-2 (compound 19) (10 mM: 1 h) inhibits the
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A648376-25mgASK1-IN-2 is a potent and orally active inhibitor of apoptosis signal-regulating kinase 1 (ASK1) , with an IC 50 of 32.8 nM. ASK1-IN-2 can be used for the research of ulcerative colitisIn VitroASK1-IN-2 (compound 19) (10 mM: 1 h) inhibits the
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A648376-50mgASK1-IN-2 is a potent and orally active inhibitor of apoptosis signal-regulating kinase 1 (ASK1) , with an IC 50 of 32.8 nM. ASK1-IN-2 can be used for the research of ulcerative colitisIn VitroASK1-IN-2 (compound 19) (10 mM: 1 h) inhibits the
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A648376-5mgASK1-IN-2 is a potent and orally active inhibitor of apoptosis signal-regulating kinase 1 (ASK1) , with an IC 50 of 32.8 nM. ASK1-IN-2 can be used for the research of ulcerative colitisIn VitroASK1-IN-2 (compound 19) (10 mM: 1 h) inhibits the